Ren Haisheng, Provorse Makenzie R, Bao Peng, Qu Zexing, Gao Jiali
Department of Chemistry and Supercomputing Institute, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Chemistry and Chemical Biology, University of California Merced , Merced, California 95343, United States.
J Phys Chem Lett. 2016 Jun 16;7(12):2286-93. doi: 10.1021/acs.jpclett.6b00915. Epub 2016 Jun 7.
Multistate density functional theory (MSDFT) is presented to estimate the effective transfer integral associated with electron and hole transfer reactions. In this approach, the charge-localized diabatic states are defined by block localization of Kohn-Sham orbitals, which constrain the electron density for each diabatic state in orbital space. This differs from the procedure used in constrained density functional theory that partitions the density within specific spatial regions. For a series of model systems, the computed transfer integrals are consistent with experimental data and show the expected exponential attenuation with the donor-acceptor separation. The present method can be used to model charge transfer reactions including processes involving coupled electron and proton transfer.
提出了多态密度泛函理论(MSDFT)来估计与电子和空穴转移反应相关的有效转移积分。在这种方法中,电荷局域化的非绝热态由Kohn-Sham轨道的块定位定义,这在轨道空间中约束了每个非绝热态的电子密度。这与约束密度泛函理论中用于在特定空间区域内划分密度的过程不同。对于一系列模型系统,计算得到的转移积分与实验数据一致,并显示出随着供体-受体间距预期的指数衰减。本方法可用于模拟电荷转移反应,包括涉及耦合电子和质子转移的过程。